HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701735Generated: October 25, 2026
Allyl Alcohol → 4-{3-[(Prop-2-en-1-yl)oxy]pyrazin-2-yl}morpholine
https://huagongshe.com/reaction/1701735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(3-Chloropyrazin-2-YL)morpholine | HCID 20528994 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 4-{3-[(Prop-2-en-1-yl)oxy]pyrazin-2-yl}morpholine | HCID 57067635 | — |
Reaction Steps
120 g of 2-chloro-3-morpholinyl-pyrazine and 70 g of allyl alcohol are dissolved in 640 ml of hexamethylphosphoric acid triamide. 28.8 g of sodium hydride are introduced into this solution over the course of 30 minutes at 0° C. The mixture is then stirred for a further hour at 0° C. and thereafter for 1 hour at 30° C. and 15 hours at room temperature, until the reaction has subsided. The reaction mixture is then poured out onto 2 liters of ice water. After the excess sodium hydride present has been decomposed, the mixture is extracted by shaking with ether. The ether extracts are washed with water until neutral, dried over sodium sulphate and evaporated in a waterpump vacuum. The residue is distilled in a high vacuum. 2-Allyloxy-3-morpholinyl-pyrazine, boiling point 105°-106° C./0.03 mm Hg, is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04195090 |
|---|
| Source dataset | uspto-grants-1980_03 |
|---|
| ORD ID | ord-4a7d77d451de4beb854b52acf32445a8 |
|---|
| Source note | uspto-grants-1980_03 |
|---|